Crossmark

A novel homozygous variant in the POLR1A gene: a complicated hereditary spastic paraplegia (c-HSP) or a hypomyelinating leukodystrophy type-27 (HLD27) phenotype?

Crossref DOI link: https://doi.org/10.1007/s10072-026-09171-5

Published Online: 2026-06-11

Published Print: 2026-07

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Tajamolian, Masoud

Ravanbod, Moez

Alavi, Shahryar

Heidari, Morteza

Rohani, Mohammad

Alavi, Afagh https://orcid.org/0000-0003-0390-2475
Funding

Funding for this research was provided by:

University of Social Welfare and Rehabilitation Sciences (3450)
License Information

Text and Data Mining valid from 2026-06-11

Version of Record valid from 2026-06-11
More Information

Article History

Received: 4 November 2025

Accepted: 6 June 2026

First Online: 11 June 2026

Declarations

:

: All authors claim absence of financial and non-financial interests.

Document is current

Any future updates will be listed below